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Quality Associate

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Proclinical

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Location:
Switzerland , Basel

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Contract Type:
Not provided

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Salary:

Not provided

Job Description:

Proclinical is seeking a Quality Associate to support quality assurance activities within a GMP environment. This role involves ensuring compliance with cGMP standards, supporting the release of GMP-relevant documents and batches, and contributing to departmental projects. You will play a key role in maintaining quality standards and supporting project-related initiatives.

Job Responsibility:

  • Review and manage GMP-relevant documents and batch records to ensure compliance
  • Provide functional expertise and support to teams within the quality assurance unit
  • Contribute to the development and implementation of quality tools, processes, and initiatives
  • Support project-related activities such as product portfolio development, quality risk assessments, training, and facility upgrades
  • Ensure adherence to internal and external quality and safety guidelines, including cGMP, SOPs, and regulatory requirements
  • Manage incoming documents, including executed batch records and vendor labels
  • Facilitate the timely release of GMP batches, labels, and investigational medical products
  • Organize, scan, file, and archive QA-owned documents, such as certificates of compliance and batch review checklists

Requirements:

  • Strong communication skills to address GMP and logistics-related queries effectively
  • Knowledge of scientific, technical, and regulatory aspects relevant to quality assurance
  • Familiarity with drug development processes and cGMP guidelines
  • Basic understanding of safety and environmental regulations
  • Good organizational skills to manage documentation and project timelines
  • Proficiency in English, both written and oral, with fluency in the site language preferred
  • Must have the right to work in this location or hold an EU passport

Additional Information:

Job Posted:
January 05, 2026

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